Home › Gyrus ACMI, LLC › UroPass
UroPass
Gyrus ACMI, LLC · Model 61054BX · UDI-DI 00821925035348
KNY
Prescription
1
510(k) clearances
392
Adverse events (2 deaths)
3
Recalls
39
Facilities
Description
UroPass Ureteral Access Sheath 10/12 Fr (3.3/4 mm) x 54 cm (5/PK)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-09-11 | Olympus Corporation of the Americas | Exposure of the UroPass product to Ultraviolet ( UV ) Radiation can cause brittleness of the device dilator tip, which may lead to broken dilator tips in the package or in patients |
| 2023-05-19 | Olympus Corporation of the Americas | Dilator tips may break in the package and in patients during surgical procedures. |
| 2011-04-15 | Gyrus Acmi, Incorporated | Gyrus ACMI, Inc. wants to bring a recall issue to their customers attention concerning one lot of their 25BX-PTFE Coated 3 cm Flexible Tip Guidewire. As a result of a manufacturin |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.